Canonical Allele Identifier: CA1845610215
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34514353A= , CM000671.2:g.34514353A= GRCh38
NC_000009.11:g.34514351A= , CM000671.1:g.34514351A= GRCh37
NC_000009.10:g.34504351A= NCBI36
NG_008127.1:g.60541A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1570-41A= MANE Select ENSP00000242317.4:n.1570-41A=
ENST00000242317.8:c.1570-41A= ENSP00000242317.4:n.1570-41A=
ENST00000442556.1:c.81-41A=
ENST00000470169.5:c.507-287A=
ENST00000485580.1:n.49-41A=
ENST00000614641.4:c.1582-41A= ENSP00000480538.1:n.1582-41A=
NM_001281428.1:c.1582-41A= NP_001268357.1:n.1582-41A=
NM_012144.3:c.1570-41A= NP_036276.1:n.1570-41A=
XM_006716758.2:c.1039-41A= XP_006716821.1:n.1039-41A=
XM_011517846.1:c.1582-41A= XP_011516148.1:n.1582-41A=
XM_011517847.1:c.1582-41A= XP_011516149.1:n.1582-41A=
XM_011517848.1:c.1324-41A= XP_011516150.1:n.1324-41A=
XM_011517849.1:c.1582-151A= XP_011516151.1:n.1582-151A=
XR_929232.1:n.1836-151A=
XR_929233.1:n.1836-151A=
XR_929235.1:n.1578-151A=
XM_006716758.3:c.1039-41A= XP_006716821.1:n.1039-41A=
XM_011517846.2:c.1582-41A= XP_011516148.1:n.1582-41A=
XM_011517847.3:c.1582-41A= XP_011516149.1:n.1582-41A=
XM_011517848.2:c.1324-41A= XP_011516150.1:n.1324-41A=
XM_011517849.2:c.1582-151A= XP_011516151.1:n.1582-151A=
XM_017014625.2:c.1312-41A= XP_016870114.1:n.1312-41A=
XR_002956774.1:n.1783-151A=
XR_929232.2:n.1783-151A=
XR_929233.2:n.1783-151A=
NM_012144.4:c.1570-41A= MANE Select NP_036276.1:n.1570-41A=
NM_001281428.2:c.1582-41A= NP_001268357.1:n.1582-41A=